Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Phosphorus containing other than solely as part of an...
Reexamination Certificate
2000-02-25
2003-02-25
Criares, Theodore J. (Department: 1614)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Phosphorus containing other than solely as part of an...
C514S126000, C514S517000, C514S707000
Reexamination Certificate
active
06525037
ABSTRACT:
FIELD OF THE INVENTION
This invention relates to a method for treating a patient suffering from atherosclerosis, or from complications caused thereby. The method involves administering an effective amount of a disulfide or thiol-containing compound to a patient suffering from atherosclerosis or from complications of atherosclerosis.
BACKGROUND OF THE INVENTION
Atherosclerosis is a common disease that stems from the build up of fatty/cholesterol plaques on the endothelial cells of arteries. The deposits mitigate thickening and stiffening of arterial tissue, with concomitant systemic or localized disorders that result from lessened blood flow. This condition often results in local ischemia, formation of thrombi, embolism due to plaque rupture, and other serious conditions, and can lead to stroke, myocardial infarction, and other life-threatening complications.
Many diverse factors, both internal and external, are thought to be responsible for the gradual onset of atherosclerosis. One of these factors is an abnormally high blood level of homocysteine. High homocysteine levels are a likely consequence of B-vitamin and/or folic acid deficiency and are also associated with reduced renal function. Often, high homocysteine levels are associated with inborn errors of amino acid metabolism.
Current methods of treating atherosclerosis depend upon the severity and location of the problem blood vessels. Particularly with the arteries of the heart, surgery is often employed to break up the deposits. Diuretics and other agents are also administered to reduce the potential serious effects of the disease.
The current methods of treating atherosclerosis carry associated risks of side effects, and are at times unsuccessful in alleviating the problem. Particularly if the underlying cause is excessive homocysteine, the deposits often recur after surgery, and many blood thinners possess potentially serious side effects as well as having no effect on the actual atheromatous deposits themselves.
Homocysteine is a transmethylated derivative of the naturally occurring amino acid methionine, a product of protein metabolism, and has the following structure-
HS—CH
2
—CH
2
—CH (NH) —COOH.
Current health literature is replete with references to the desirability of lowering plasma levels of homocysteine. Many publications suggest that homocysteine levels can be safely reduced by increased intake of B-vitamins and folic acid.
Mesna (sodium 2-mercaptoethene sulfonate) and dimesna (disodium 2,2′-dithiobis ethane sulfonate) are known therapeutic compounds that have heretofore demonstrated a wide variety of therapeutic uses. Both mesna and dimesna have been shown to be effective protective agents against certain specific types of toxicity associated with the administration of cytotoxic drugs used to treat patients for various types of cancer.
In particular, mesna has been used with some success in mitigating the toxic effects of cytotoxic agents such as ifosfamide, oxazaphosphorine, melphalane, cyclophosphamide, trofosfamide, sulfosfamide, chlorambucil, busulfan, triethylene thiophosphamide, triaziquone, and others, as disclosed in U.S. Pat. No. 4,220,660, issued Sept. 2, 1980.
The near absence of toxicity of dimesna further underscores the usefulness of this compound, as large doses can be given to a patient without increasing the risk of adverse effects from the protective agent itself.
Further, pharmacological profiles of each compound indicate that, if proper conditions are maintained, mesna and dimesna do not prematurely inactivate primary therapeutic drugs to a significant degree. Thus, neither compound will significantly reduce activity of the chemotherapeutic agent, and in many cases, act to potentiate the effect of the main drug on targeted cancer cells.
The molecular structures of both mesna and dimesna are shown below as Structure I and Structure II respectively.
HS—CH
2
—CH
2
—SO
3
Na (I)
NaSO
3
—CH
2
—CH
2
—S—S—CH
2
—CH
2
—SO
3
Na (II)
As shown, dimesna is a dimer of mesna, with the optimum conditions for oxidation occurring in the slightly basic (pH ~7.3), oxygen rich environment found in blood plasma. In mildly acidic, low oxygen conditions, in the presence of a reducing agent such as glutathione reductase, conditions prevalent in the kidneys, the primary constituent is mesna.
Mesna acts as a protective agent for a number of cytotoxic agents by substituting a nontoxic sulfhydryl moiety for a toxic hydroxy (or aquo) moiety. This action is particularly evidenced in the coadministration of mesna and oxazaphosphorine, and in the administration of dimesna along with certain platinum agents and/or taxanes.
Dimesna, as well as some analogues, have excellent toxicity profiles in mammalian species. In fact, dimesna has been administered intravenously to mice and dogs in doses higher than the accepted oral LD
50
for common table salt (3750 mg/kg) , with no adverse effects. Dimesna has also been administered to humans in doses exceeding 40 g/m
2
, with no adverse effects.
Mesna, and other analogues with free thiol moieties, constitute the more physiologically active form of the two types of compounds described in this specification. These compounds manifest their activity by providing free thiol moieties for terminal substitution at locations where a terminal leaving group of appropriate configuration, usually a hydroxy, aquo or superoxide is located. Mesna also tends to form conjugates with naturally occurring biochemicals that contain a free thiol moiety, such as cysteine, glutathione, homocysteine, and others.
Dimesna and other disulfides can be activated intracellularly by glutathione reductase, a ubiquitous enzyme, thereby generating high concentrations of intracellular free thiols. These free thiols act to scavenge the free radicals and other nucleophilic compounds often responsible for causing cell damage.
This profile is especially significant in explaining the success of dimesna in controlling and mitigating the toxic effects of platinum complex antitumor drugs. The mechanism for action in the case of cisplatin (cis-diammine dichloro platinum) is explained in U.S. Pat. No. 5,789,000, which is incorporated herein by reference.
Mesna, dimesna, and analogues of these compounds have been the subject of several prior pharmaceutical uses described in the literature and in prior patents, both in the United States and around the world. In addition to the cytotoxic agent protection uses, one or more of these compounds have proven effective, in vitro, against a multiplicity of biological targets, and have been effective, in vivo, in the treatment of sickle cell disease, radiation exposure, chemical agent exposure, and other uses.
Mesna, dimesna, and analogues thereof are synthesized from commonly available starting materials, using acceptable routes well known in the art. One such method involves the two-step, single pot synthetic process for making dimesna and like compounds of the following formula:
R
1
—S—R
2
;
wherein:
R
1
is hydrogen, X-lower alkyl, or X-lower alkyl-R
3
;
R
2
is -lower alkyl-R
4
;
R
3
and R
4
are each individually SO
3
M or PO
3
M
2
;
X is absent or X is sulfur; and
M is an alkali metal.
The process essentially involves a two-step single pot synthetic process, which results in the conversion of an alkenyl sulfonate salt or acid to the desired formula I compound. The process in the case of mesna is a single step process that converts the alkenyl sulfonate salt to mesna or a mesna derivative by reacting with an alkali metal sulfide or with hydrogen sulfide.
If the desired end product is dimesna or a dimesna analogue, a two-step single pot process is involved. Step 1 is as described above. Step 2 of the process is performed in the same reaction vessel as Step 1 without the need to purify or isolate the mesna formed during that step. Step 2 includes the introduction of oxygen gas into the vessel, along with an increase in pressure and temperature above ambient values, at least 20 pounds per square inch (psi) and at least 60° C. Dimesna or a derivative t
Hausheer Frederick H.
Peddaiahgari Seetharamulu
BioNumerik Pharmaceuticals, Inc.
Dodd Thomas J.
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